Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE Healthcare, LLC Due to Patient monitors may restart due to network overload...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare, LLC directly.
Affected Products
B20i Patient Monitor and B20i V2 Patient Monitor. The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and during intra-hospital transport.
Quantity: 6,458 patient monitors
Why Was This Recalled?
Patient monitors may restart due to network overload caused by network configuration.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report